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A Nicholson

Showing results (971-980 of 1,065) with videos related to

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Annals of Neurology|February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesisM J Smith, J B Kwok, C A McLean, et al.
Human Molecular Genetics|January 9, 2013
A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) geneMarina L Kennerson, Eppie M Yiu, David T Chuang, et al.
Neuroscience Letters|October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in AustraliaK Taddei, D Yang, C Fisher, et al.
Biology Open|September 8, 2018
Neuronal cell culture from transgenic zebrafish models of neurodegenerative diseaseJamie R Acosta, Maxinne Watchon, Kristy C Yuan, et al.
Human Brain Mapping|July 14, 2018
Intrinsic connectivity network dynamics in PTSD during amygdala downregulation using real-time fMRI neurofeedback: A preliminary analysisAndrew A Nicholson, Daniela Rabellino, Maria Densmore, et al.
BMC Neurology|August 30, 2008
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9Agnes A Luty, John B J Kwok, Elizabeth M Thompson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2017
Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1André B Rietman, Thijs van der Vaart, Ellen Plasschaert, et al.
European Journal of Psychotraumatology|June 19, 2025
Identity in turmoil: Investigating the morally injurious dimensions of minority stressAndrew A Nicholson, Sandhya Narikuzhy, Jakub Wolf, et al.
Neurobiology of Aging|February 14, 2021
Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosisSandrine Chan Moi Fat, Emily P McCann, Kelly L Williams, et al.
Clinical and Experimental Immunology|April 6, 2005
A transgenic mouse model for studying the clearance of blood-borne pathogens via human complement receptor 1 (CR1)A Repik, S E Pincus, I Ghiran, et al.
Pageof 107

Showing results (971-980 of 1,065) with videos related to

Sort By:
Pageof 107
Annals of Neurology|February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesisM J Smith, J B Kwok, C A McLean, et al.
Human Molecular Genetics|January 9, 2013
A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) geneMarina L Kennerson, Eppie M Yiu, David T Chuang, et al.
Neuroscience Letters|October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in AustraliaK Taddei, D Yang, C Fisher, et al.
Biology Open|September 8, 2018
Neuronal cell culture from transgenic zebrafish models of neurodegenerative diseaseJamie R Acosta, Maxinne Watchon, Kristy C Yuan, et al.
Human Brain Mapping|July 14, 2018
Intrinsic connectivity network dynamics in PTSD during amygdala downregulation using real-time fMRI neurofeedback: A preliminary analysisAndrew A Nicholson, Daniela Rabellino, Maria Densmore, et al.
BMC Neurology|August 30, 2008
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9Agnes A Luty, John B J Kwok, Elizabeth M Thompson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2017
Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1André B Rietman, Thijs van der Vaart, Ellen Plasschaert, et al.
European Journal of Psychotraumatology|June 19, 2025
Identity in turmoil: Investigating the morally injurious dimensions of minority stressAndrew A Nicholson, Sandhya Narikuzhy, Jakub Wolf, et al.
Neurobiology of Aging|February 14, 2021
Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosisSandrine Chan Moi Fat, Emily P McCann, Kelly L Williams, et al.
Clinical and Experimental Immunology|April 6, 2005
A transgenic mouse model for studying the clearance of blood-borne pathogens via human complement receptor 1 (CR1)A Repik, S E Pincus, I Ghiran, et al.
Pageof 107